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A number of novel imidazophenoxazine-4-sulfonamides have been designed as potential inhibitors of PDE4.
A series of thiadiazole derivatives has been designed as potential allosteric, substrate competitive inhibitors of the protein kinase JNK.
A new class of compounds based on S-benzylated guanylthiourea has been designed as potential PfDHFR inhibitors using computer aided methods (molecular electrostatic potential, molecular docking).
A number of novel 1- 3-arylprop-2-ynyl) substituted 1- 3-arylprop-2-ynyl derivatives related to nimesulide and their 2-oxo analogues have been designed as potential inhibitors of PDE4.
A number of novel 1,8-disubstituted 5,5-dimethyl-4,5-dihydro-1H-benzo[g]indazoles based on a conformationally restricted pyrazole framework have been designed as potential inhibitors of PDE4.
In continuation of our project related to the syntheses of pharmacologically important heterocycles, a new series of chromone thiazole hybrids have been designed as potential ligands for human adenosine receptors.
Similar(51)
Heteroarylalanine derivatives 4 were designed as potential inhibitors of neutral endopeptidase (NEP EC 3.4.24.11).
Hybrid compounds containing hydrazones and benzofuroxan pharmacophores were designed as potential Trypanosoma cruzi-enzyme inhibitors.
Novel N-indolylmethyl substituted spiroindoline-3,2′-quinazolines were designed as potential inhibitiors of SIRT1.
Novel thieno[3,2-c]pyran-4-one based small molecules were designed as potential anticancer agents.
The 2,2,4-trimethyl-1,2-dihydroquinolinyl substituted 1,2,3-triazole derivatives were designed as potential inhibitors of PDE4B.
More suggestions(15)
been named as potential
been recommended as potential
been designed as imaginary
been accepted as potential
been introduced as potential
been floated as potential
been investigated as potential
been dismissed as potential
been chosen as potential
been analyzed as potential
been synthetized as potential
been recognized as potential
been reported as potential
been regarded as potential
been touted as potential
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